Review: Etidronate decreases vertebral but not nonvertebral fractures in postmenopausal womenPDF
ACP J Club. 2002 May-June;136:98. doi:10.7326/ACPJC-2002-136-3-098
Cranney A, Welch V, Adachi JD, et al. Etidronate for treating and preventing postmenopausal osteoporosis. Cochrane Database Syst Rev. 2001;(4):CD003376 (latest version 25 Mar 2001). [PubMed ID: 11687195]
In postmenopausal women, is etidronate effective and safe for treating postmenopausal osteoporosis and preventing fractures?
Studies were identified by searching MEDLINE, HealthSTAR, EMBASE/Excerpta Medica, and Current Contents (1966 to 1998) with terms that include etidronate, osteoporosis, postmenopausal, diphosphonates, and bisphosphonates. Conference abstracts were hand searched, references of relevant articles were scanned, and experts were contacted.
Published and unpublished studies were selected if they were randomized controlled trials (RCTs) of ≥ 1 year of duration in postmenopausal women; compared etidronate (using the intermittent cyclic method at 400 mg/d for 14 to 20 d, and then using calcium or vitamin D, or both) with placebo, calcium, vitamin D, or calcium plus vitamin D; and evaluated outcomes of fracture reduction, change in bone mineral density (BMD), or toxicity.
Data were extracted on participants, treatment type and duration, outcomes, method of densitometry, and methodologic quality.
13 RCTs (1267 women), 9 (1010 women) of which reported vertebral fractures, met the selection criteria. 5 trials included women with established osteoporosis, and 8 trials included early postmenopausal women without osteoporosis. All studies ensured allocation concealment, and 12 used an intention-to-treat analysis. 6 trials were blinded, and 7 were unblinded.
At 2 years, etidronate reduced vertebral fractures but had no effect on nonvertebral fractures or hip fractures alone (Table). At 3 years, etidronate was associated with greater percentage changes in BMD than was placebo at the lumbar spine (risk difference [RD] 4.3%, 95% CI 2.7% to 5.9%), at the femoral neck (RD 2.19%, CI 0.4% to 3.95%), and for the total body (RD 0.97%, CI 0.4% to 1.6%) but not at the distal forearm (RD 0.43%, CI −1.6% to 2.5%). Etidronate and placebo did not differ for the number of overall withdrawals.
In postmenopausal women, etidronate safely increases bone mineral density and decreases vertebral fractures but has no effect on nonvertebral or hip fractures.
Source of funding: Not stated.
For correspondence: Dr. A. Cranney, Ottawa Hospital, Ottawa, Ontario, Canada. E-mail email@example.com.
Table. Etidronate vs placebo in postmenopausal women at 2 years*
|Outcomes||Weighted event rates||RRR (95% CI)||NNT (CI)|
|Vertebral fractures||5.9%||10%||40% (12 to 59)||25 (14 to 91)|
|Nonvertebral fractures||11.1%||11.3%||2% (−42 to 32)||Not significant|
|Hip fractures||1.7%||1.4%||20% (−63 to 288)||Not significant|
*Abbreviations defined in Glossary; RRR, RRI, NNT, NNH, and CI calculated from data in article using a fixed-effects model.
In this well-done meta-analysis, Cranney and colleagues confirmed that postmenopausal women taking etidronate for at least 2 years have higher bone mineral density and a lower risk for vertebral fractures than do those taking placebo. Studies comparing etidronate with hormone replacement therapy, calcitriol, or calcitonin and studies of men and patients with steroid-induced osteoporosis were not included in this review.
The reduction in risk for vertebral fractures with etidronate appears to be slightly less than that with alendronate or risedronate (which have about a 50% risk reduction) and similar to that observed with raloxifene (1−3). However, no head-to-head comparisons of these agents are available.
In RCTs, only alendronate and risedronate reduce the risk for nonspinal and hip fractures, which suggests that etidronate could be used for women in their middle menopausal years (55 to 65 y) who are at high risk for vertebral fracture. Raloxifene would also be appropriate for this population. Among older women (> 65 y) who are at risk for hip fractures, use of alendronate or risedronate should be considered.
Although this meta-analysis has clarified the role of etidronate in the prevention and treatment of postmenopausal osteoporosis, some contentious areas relating to the use of bisphosphonates still exist, including the optimal duration of use and the effect on fracture risk when the bisphosphonate is stopped. How etidronate compares with other antiresorptives and the efficacy of etidronate in men also require further study.
Sophie Jamal, MD
Women’s College Hospital
Toronto, Ontario, Canada
1. Black DM, Cummings SR, Karpf DB, et al. Randomised trial of effect of alendronate on risk of fracture in women with existing vertebral fractures. Lancet. 1996;348:1535-41. [PubMed ID: 8950879]
2. Harris ST, Watts NB, Genant HK, et al. Effects of risedronate treatment on vertebral and nonvertebral fractures in women with postmenopausal osteoporosis: a randomized controlled trial. JAMA. 1999;282:1344-52. [PubMed ID: 10527181]
3. Ettinger B, Black DM, Mitlak BH, et al. Reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: results from a 3-year randomized clinical trial. JAMA. 1999;282:637-45. [PubMed ID: 10517716]